HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

Hydrochloric Acid → HCID 131713413, compound

HRID 1903247
Notes
Print preview

Reaction equation

HRID 1903247 reaction equation
[F:1][CH:2]([F:25])[CH:3]([NH:17][CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[CH2:4][CH2:5][N:6]1C(=O)C2=CC=CC=C2C1=O.[ClH:26]>>[ClH:26].[ClH:26].[F:1][CH:2]([F:25])[CH:3]([NH:17][CH2:18][C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1)[CH2:4][CH2:5][NH2:6]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 313Hydrochloric AcidHCID 20468458HCID 20468458, compound

Product 1

HCID 131713413HCID 131713413, compound

Conditions

Temperature
110 °C

Procedure

A solution of N-(4,4-difluoro-3-benzylaminobutyl) phthalimide (0.585 g, 1.72 mM) prepared as in Step D in concentrated hydrochloric acid (50 ml) is heated at 110° C. for 15 hours. The solvent is evaporated in vacuo, and the residue is taken up in cold water (50 ml). The aqueous phase is filtered and concentrated in vacuo, washed three times with diethyl ether, and then evaporated to dryness. The oily residue is triturated several times with isopropanol. The solvent is removed in vacuo yielding a white foam: 0.490 g (quantitative yield) of the required compound.

Workup

custom
The solvent is evaporated in vacuo
  • filtrationThe aqueous phase is filtered
  • concentrationconcentrated in vacuo
  • washwashed three times with diethyl ether
  • customevaporated to dryness
  • customThe oily residue is triturated several times with isopropanol
  • customThe solvent is removed in vacuo
  • customyielding a white foam
  • Sources & evidence

    ORD record
    ord-6647d4f12489491da1da267dc1bdf51e
    Source dataset
    uspto-grants-1984_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US04435425

    Reaction notes

    Loading…

    On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes